dextro,laevo-tryptophan
propionic acid, 2-amino-3-indol-3-yl-

Sponsors

Name: 2-amino-3-(1H-indol-3-yl)propanoic acid
CAS Number: 54-12-6Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 200-194-9
Nikkaji Web: J314.694D
Beilstein Number: 86196
MDL: MFCD00064339
XlogP3: -1.10 (est)
Molecular Weight: 204.22904000
Formula: C11 H12 N2 O2
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: cosmetic agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 230.00 °C. @ 760.00 mm Hg
Boiling Point: 447.90 °C. @ 760.00 mm Hg (est)
Flash Point: 436.00 °F. TCC ( 224.70 °C. ) (est)
logP (o/w): 1.040 (est)
Soluble in:
 water, 2848 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: antistatic agents
hair conditioning
masking agents
 
Suppliers:
George Uhe Company
DL-Tryptophan
Glentham Life Sciences
DL-Tryptophan
Penta International
DL-TRYPTOPHAN, Kosher
Santa Cruz Biotechnology
For experimental / research use only.
DL-Tryptophan 99%
Sigma-Aldrich: Aldrich
For experimental / research use only.
DL-Tryptophan ≥99%
 
Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intraperitoneal-mouse LD50 > 1000 mg/kg
Biochemical Pharmacology. Vol. 15, Pg. 2134, 1966.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: cosmetic agents
Recommendation for dextro,laevo-tryptophan usage levels up to:
 not for fragrance use.
 
Recommendation for dextro,laevo-tryptophan flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
ClinicalTrials.gov: search
Daily Med: search
Chemical Carcinogenesis Research Information System: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA GENetic TOXicology: Search
Env. Mutagen Info. Center: Search
EPA Substance Registry Services (TSCA): 54-12-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 1148
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 1
 2-amino-3-(1H-indol-3-yl)propanoic acid
Chemidplus: 0000054126
RTECS: YN6129200 for cas# 54-12-6
 
References:
 2-amino-3-(1H-indol-3-yl)propanoic acid
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 54-12-6
Pubchem (cid): 1148
Pubchem (sid): 134971646
 
Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
Golm Metabolome Database: Search
KEGG (GenomeNet): C00806
HMDB (The Human Metabolome Database): HMDB30396
FooDB: FDB002251
Export Tariff Code: 2933.90.1000
MedlinePlusSupp: View
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
 antistatic agents 
 
Occurrence (nature, food, other): note
 found in nature
 
Synonyms:
 alanine, 3-indol-3-yl-
2-amino-3-(1H-indol-3-yl)-propionicacid
2-amino-3-(1H-indol-3-yl)propanoic acid
(±)-2-amino-3-(3-indolyl)propionic acid
2-amino-3-(lH-indol-3-yl)-propanoic acid
2-amino-3-indol-3-ylpropionic acid
DL-a-amino-3-indolepropionic acid
2-amino-3-indolylpropanic acid
2-amino-3-indolylpropanoic acid
a-aminoindole-3-propionic acid
 indole-3-propionic acid, a-amino-
 propionic acid, 2-amino-3-indol-3-yl-
(±)-tryptophan
(RS)-tryptophan
DL-tryptophan
 tryptophan, DL-
 tryptophane
DL-trytophan
 
 
Notes:
Dietary supplement, nutrient Tryptophan is one of the 20 standard amino acids, as well as an essential amino acid in the human diet. Only the L-stereoisomer of tryptophan is used in structural or enzyme proteins, but the D-stereoisomer is occasionally found in naturally produced peptides (for example, the marine venom peptide contryphan). (Wikipedia)
 
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